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(11) | EP 1 011 357 B1 |
| (12) | EUROPEAN PATENT SPECIFICATION |
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METHOD OF MAKING INJECTION MOLDED ORTHOTICS VERFAHREN ZUM SPRITZGIESSEN EINER ORTHESE PROCEDE D'INJECTION D'ORTHESE MOULEE PAR INJECTION |
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| Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice to the European Patent Office of opposition to the European patent granted. Notice of opposition shall be filed in a written reasoned statement. It shall not be deemed to have been filed until the opposition fee has been paid. (Art. 99(1) European Patent Convention). |
Background of the Invention
Field of the Invention
[0001] The present invention relates generally to orthopedic appliances. More particularly, the invention concerns a novel method for making injection molded, finished functional orthotics by using various critical measurements made of the patient's feet.
Discussion of the Prior Art
[0002] Orthopedic appliances, or foot supports, having various shapes and configurations have been known for many years. The prior art'appliances range from simple foam, leather, cork, or sponge rubber arch supports that can be purchased in drugstores to sophisticated, custom-fitted orthotics formed of various rigid or semirigid materials. These latter devices, while much more effective than the former, are typically quite expensive and are generally constructed by orthopedic laboratories in accordance with detailed prescriptions provided by the examining doctor.
[0003] Generally speaking, the primary function of an orthotic is to correctly limit the complex motions of excessive pronation and supination. Pronation may be simply described as the flattening or rolling inward of the foot as the foot strikes the ground as during walking or running. Excessive pronation can cause the tibia and fibula to rotate inwardly sometimes placing severe strain on the leg muscles. Supination, on the other hand, is the rolling outward of the foot during walking or running. When either of these motions become excessive, painful damage to the knees, ankles and feet can occur.
[0004] In making the more sophisticated functional orthotics, the conventional practice, which has remained essentially, unchanged for many years, is to first make an impression of the patient's foot. This impression, which may be made in plaster of paris or in a crushable, foam-like material, is forwarded to the orthopedic laboratory along with the examining doctor's instructions. One method of making the impression, or negative depression, using foam blocks is described in U.S. Patent No. 3,320,347 issued to Greenawalt. This method, as described by Greenawalt, comprises placing a foam block on the floor, centering one of the patient's feet relative to the block and then having the patient stand so that his weight is equally divided on both feet. As the patient's weight is placed on the foam block, the foam cells of the block will be crushed and a negative impression of the patient's foot will be created.
[0005] The thrust of the Greenawalt method is to use the impression made in the crushable foam block to make various measurements, visual observations and touch evaluations which serve as the basis for constructing the corrective arch support. For example, measurements are made of the length and width of the impression and observations of the position of the metatarsal heads, of plantar abnormalities in the inner and outer longitudinal arch and of the presence and degree of supination are made. These measurements and observations are then used in laying out the dimensions and sizes of the leather blanks which are to be used for constructing the corrective arch support.
[0006] Another prior art approach followed by many orthopedic laboratories in constructing functional orthotics involves pouring a solution of plaster of paris into the impression, or negative depression, to make an uncorrected replica or cast of the patient's foot. This having been done, the uncorrected replica which provides an exact duplication or the contours of the lower surface of the patient's foot, is corrected in the manner proscribed by the examining doctor. For example, the uncorrected replica is often wedged or adjusted to simulate the position of the foot in the neutral position or in the position which the doctor wishes to control foot function. The neutral position of the foot is the position wherein the foot is neither supinated nor pronated and the midtarsal joint is maximally pronated. In this neutral position, the foot typically transfers force most effectively. In biomechanical terms the foot must ideally absorb the force of gravity at heel contact and then create a rigid lever to correctly propel the body forward for the next step. When the foot is not in or near the neutral position, it cannot: absorb force nor can it create an effective lever for propelling the body forward in a proper manner. Such a problem can cause the foot structure to break down and, over time, lead to severe neck pain, back pain, foot pain, bunions, heel spurs, and the like.
[0007] The wedging step involves first bisecting the posterior aspect of the calcaneus and then wedging the cast until this bisection is generally perpendicular to the horizontal plane. The wedging, per se, is generally accomplished by adding a plaster forefoot platform to the cast. Preferably, the platform extends from about one centimeter proximal to the first metatarsal head and the fifth metatarsal head to the sulcus area and spans the positive mold from the medial aspect (outside edge of first toe) to the lateral aspect (outside edge of fifth toe).
[0008] Typically, the wedged mold is then further modified with a plaster of paris buildup to account for fat pad expansion around the heel and along the lateral foot border, to allow for compression of the medial arch and transverse arch, and to create a smooth transition from the forefoot platform to the arch and midfoot.
[0009] It is apparent from the foregoing that the method for correcting the uncorrected replica is a complex, time-consuming, and highly labor intensive operation. Further, the prior art method is somewhat imprecise and is highly dependent on the skill of the particular technician involved.
[0010] Although the same basic principles are used by the laboratory technician to correct the uncorrected replica formed from the impression of the patient's foot, experience has shown that no two people will correct a particular replica in exactly the same way. Thus, if two identical uncorrected replicas were to be sent to two different orthopedic laboratories, the orthotic returned to the doctor would be different in various respects. This is because the laboratory technician who makes the corrections is of necessity required to make various subjective decisions based upon his own experience and capabilities. For example, no two feet are the same length and width, even on the same patient. Nevertheless the examining doctor, or other licensed professional, typically wants the two orthotics made for the same patient to look symmetrical. Accordingly, the technician is forced to subjectively judge where the forefoot platforms should be located and how much expansion should be placed on each foot. No two technicians or laboratories will make the same decisions in the same way.
[0011] Further contributing to the impreciseness of the prior art techniques for making functional orthotics is the method of forming the orthotic from the corrected replica. Basically, this method involved thermal forming of a layer of polyolefin plastic sheet over the lower surface of the corrected replica. If the forming step is correctly done and the polyolefin sheet is properly heated and cooled, the upper surface of the sheet will correspond substantially to the lower surface of the corrected replica. One such method of thermal forming is described in U.S. Patent No. 4,702,255 issued to Schenkel. However, if the forming step is incorrectly done, precise replication of the lower surface of the corrected replica will not result.
[0012] For the foregoing reasons, the products made by different laboratories are somewhat different and even the corrections made within a single laboratory may be different from foot to foot. Further contributing to deficiencies in prior art orthotics is the absence of reliable methods for analyzing the patient's foot impressions and the inability of a given orthotic constructed from the impression to, in fact, properly control the patient's foot.
[0013] From an exhaustive study made by the present inventor of literally thousands of orthotics made in accordance with the prior art processes discussed in the preceding paragraphs, a most surprising discovery was made. Since the conventional wisdom has been that the foot of each patient is unique with no two feet being alike, those working in the field have presumed that no two orthotics made by the previously discussed prior art process would be alike. Surprisingly, the studies made by the present inventor indicate that this, in fact, is not the case. These studies included the careful measurement of the contour of each of a large number of uncorrected replicas presented for correction followed by the careful measurement of the corrected contour of each corrected replica produced in the laboratory in accordance with the processes described in the preceding paragraphs. An analyses of the measurements showed that, while the uncorrected replicas typically varied in certain respects, many of the corrected replicas and the orthotics formed therefrom were nearly functionally identical and fell into rather well defined groups.
[0014] Based on the discovery that families of different, but related uncorrected replicas, when corrected by traditional processes, produced nearly identical corrected replicas, the present inventor reasoned that a permanent corrected replica in the nature of a male-forming master, could be constructed and used repeatedly to form final orthotics for each of these identical families. In this way, the substantial amount of labor required to correct each replica of the group of uncorrected replicas which made up the family could be avoided. Continuing studies by the inventor of additional uncorrected replicas received by the laboratory enabled the identification of a large number of identifiable groups of uncorrected replicas which, when corrected, would produce a substantially functionally identical finished orthotic. This information then made it possible to construct a number of forming masters for each of the identified families. After a large inventory of forming masters were then constructed, the next step in the development was to analyze each new uncorrected replica received by the laboratory and identify it with one of the previously identified families of uncorrected replicas which, when corrected, would produce a virtually identical finished orthotic. The forming master associated with the identified family was then used to form the finished orthotic for the newly received uncorrected replica rather than laboriously constructing a corrected replica and using it to form the finished orthotic for the patient.
[0015] The approach to making finished orthotics described in the preceding paragraphs was successfully commercialized and the orthotics made by the process were marketed by KLM Laboratories, Inc., of Valencia, California, under the name and style "SYSTEM RX". While this novel process was less labor intensive than the traditional prior art process whereby each uncorrected replica was corrected and then used to form the finished orthotic, the many processing difficulties and substantial labor involved in high temperature forming of the orthotic from a selected one of the male-forming molds remained. In a manner presently to be described, the methods of the present invention elegantly avoids the difficult, costly and time consuming step of high temperature forming and finishing of the orthotics from the male-forming masters and produces even a higher quality finished product at a significantly lower cost.
[0016] Before discussing the details of the present invention, it should be pointed out that others working in the field have also devised means for reducing the labor costs involved in the hand correction of each of the uncorrected replicas received by the processing laboratory. One such approach is disclosed in U.S. Patent No. 5,054,148 issued to Grumbine. The Grumbine process involves the use of a computer-controlled mill 1 to produce each individual orthotic from a monolithic workpiece. In accordance with the process, the specific contour of the top and bottom surface of an orthotic for a particular patient is first described and stored in terms of x, y, z coordinates and subsequently formatted such that a particular x, y, z coordinate, i.e. a specific longitudinal and lateral position on a workpiece yields a particular height (z) positioning of the machine tool. The machine tool is then guided along parallel paths through the workpiece while the machine tool's height is automatically adjusted to conform with the desired surface contour.
[0017] Although the Grumbine process and other somewhat similar prior art, computer-controlled milling operations developed by others working in the field have proven generally satisfactory, a considerable investment in sophisticated tooling such as scanners, computers and large computer-controlled milling machines is required. In addition, each order requires a unique set up and milling process which increases the overall cost per order.
[0018] Another prior art approach to making custom-made shoe inserts is described in U. S. Patent No. 4, 876, 758 issued to Rolloff et al. This patent discloses a foot impression unit which is provided with an array of gauging elements, a control mechanism for urging the gauging elements into contact with the undersurface of a person's foot to form an impression of the undersurface of the foot and a sensing mechanism for scanning the gauging elements to produce digital signals indicative of the positions of the gauging elements. These digital signals are stored and processed by a computer to provide a stored data record serving as a digital representation of the impression of the undersurface of the foot. The computer may also be employed to provide stored additional information for modifying that data record to compensate for a perceived defect of the foot with the x, y, z information derived. Once again, the custom-made shoe insert is made by a conventional computer controlled milling machine using the stored data for a particular patient. Once again, each order requires expensive and time consuming set-up and milling operations.
[0019] As will be better understood from the discussion which follows, the methods of the present invention uniquely overcome most of the drawbacks of the prior art processes for producing orthotics by providing a fast, accurate, efficient, and non-labor intensive injection molding process for making high quality precision orthotics in very high volumes.
Summary of the Invention
[0021] By way of brief summary, one form of the method for making an injection molded orthotic involves first selecting a multiplicity of uncorrected replicas of the human foot, each of which is to be later modified to create a corrected replica. The contoured lower surface of each uncorrected replica of the multiplicity of uncorrected replicas selected is then analyzed to identify thereon a multiplicity of x, y coordinates. This done, the contoured surface is spaced apart from a reference plane and for each x, y coordinate identified thereon, the distance between the coordinate and the reference plane, that is the z coordinate, is determined and recorded to develop a first set of x, y, z coordinate data. The x, y, z coordinate data thus developed defines the topography of the lower surface of the patient's foot as replicated by the uncorrected replicas which were produced from negative casts taken by the examining doctor of the patient's foot. In an alternate method, the details of which will, later be discussed, the negative casts received from the doctor, rather than the uncorrected replicas, are analyzed to develop the first set of x, y, z data.
[0022] Following the correction by traditional methods of the uncorrected replicas, each of the corrected replicas thus formed is used to produce a functional orthotic. Each of the finished orthotics thus produced is then studied to identify those finished orthotics that are substantially functionally identical. The substantially identical finished orthotics are then grouped into a plurality of discreet, finished orthotic groups. Once these groups of finished orthotics are determined and appropriately identified, an injection mold for each family is constructed. The injection mold for each family is carefully constructed so that the internal cavity of the mold, when filled with a moldable plastic will produce a finished orthotic that is substantially identical to the plurality of finished orthotics which make up the particular group that was identified. By reviewing the recorded data, it can be easily ascertained which uncorrected replicas were used to produce the corrected replicas and which finished orthotics were made from these correct replicas. It follows that each injection mold can then be identified with the particular group of uncorrected replicas from which the finished orthotic was derived. In this regard, for each group of uncorrected replicas, the x, y, z coordinate data corresponding to that group is identified and recorded and, in this way, a plurality of groups of x, y, z comparison data are developed. Each group of x, y, z comparison data is then identified with a particular injection mold.
[0023] Once each of the injection molds is associated with a particular comparison group, a newly received uncorrected replica can be analyzed and identified with a particular mold by comparing the x, y, z data of the uncorrected replica with the x, y, z comparison data to determine the group with which it is most closely associated. Once this is done, the proper mold can be selected. Then, using this mold, a precise orthotic can readily be constructed for use by the patient. In actual practice, matching of the patient with the proper comparison x, y, z data group is accomplished by first developing x, y, z data for the contoured lower surface of the patient's foot. This patient x, y, z data is then compared with the earlier defined and tabulated comparison group data to identify the particular comparison group within which the patient x, y, z data falls. It is then a simple matter to identify the particular injection mold which corresponds to the selected group of comparison x, y, z data and to use that injection mold to produce the finished orthotic for the particular patient.
[0024] An alternate method of the invention for developing comparison x, y, z data which can be used to select the correct injection mold for a given patient involves the careful analysis of the corrected replicas formed by traditional methods from the uncorrected replicas made using the impression provided by the examining doctor. More particularly, in accordance with this alternate method of the invention, the contoured lower surface of each corrected replica is analyzed to identify thereon a multiplicity of x, y coordinates. This done the contoured surface of the corrected replica is spaced apart from a referred plane and the distance between the reference plane and each of the x, y coordinates is determined and recorded to develop a second set of x, y, z coordinate data. This second set of x, y, z data substantially defines the topography of the lower surface of the corrected replica, and reflects the corrections prescribed by the examining doctor that are believed necessary to properly control the foot functions of the particular patient.
[0025] After creating the second set of x, y, z coordinate data, this data is studied to identify those corrected replicas that are substantially identical. This done the substantially identical corrected replicas are grouped into a plurality of discreet, corrected replica families. Once these families of corrected replicas are determined and appropriately identified, an injection mold for each family is constructed. The injection mold for each family is carefully constructed so that the internal cavity of the mold, when filled with a moldable plastic will produce a finished orthotic which is substantially identical to the plurality of finished orthotics formed using the particular family of corrected replicas. By reviewing the recorded data, it can be easily ascertained which uncorrected replicas were used to produce the corrected replicas and the finished orthotics made therefrom which make up each family. It follows then that, as before, each injection mold can be identified with the particular group of uncorrected replicas which, when corrected, produces the finished orthotic that corresponds to the orthotic produced by the particular injection mold. Once the particular group of uncorrected replicas is identified, the x, y, z, data corresponding to that group is identified and the plurality of groups of comparison x, y, z data can be developed.
[0026] With the foregoing in mind, it is a primary object of the present invention to provide a method of making, through use of an injection mold, a functional orthotic that is a quality equal to or better than that of a functional orthotic made from a corrected replica that is constructed by conventional prior art techniques from an uncorrected replica of the patient's foot.
[0027] Another object of the invention is to provide a method of the aforementioned character in which the prescription data typically provided by the examining doctor can be used to quickly and easily identify a particular injection mold that will produce a finished orthotic that is substantially identical to that which would have been heat formed from a corrected replica of the patient's foot that was made by conventional prior art techniques.
[0028] Another object of the invention is to provide a method of making a plurality of specially configured injection molds which can be used repeatedly to produce high quality, functional orthotics for virtually every type of problem for which functional orthotics are prescribed by an examining doctor.
[0029] Another object of the invention is to provide a method as described in the preceding paragraphs in which a definition of the contour of the patient's foot, provided either by means of a negative or positive replica of the patient's foot, or by other contour data obtainable by scanning techniques, or the like, can be used to quickly and easily select the proper injection mold to be used in making an orthotic for a particular patient.
[0030] Still another object of the invention is to provide a method of making precision functional orthotics by injection molding techniques, which techniques, are considerably more efficient and substantially less labor intensive than presently practiced, prior art techniques.
[0031] Yet another object of the invention is to provide a method of making precision, high-quality functional orthotics on an as-needed basis from a patient's foot contour data that is on file even in the absence of the original impression of the patient's foot, and in the absence of a corrected replica of the patient's foot.
Brief Description of the Drawings
[0032]
Figure 1 is a generally perspective view of one form of functional orthotic produced in accordance with the method of the invention.
Figure 2 is a plan view of the lower surface of a corrected replica, which is formed by traditional methods from the uncorrected replica which replicates the lower surface of the foot of the patient. Exemplary x, y coordinates used to identify the surface contour are indicated in the drawing.
Figure 3 is a generally perspective view of the corrected replica shown in Figure 2, the contoured surface of which is spaced apart from a reference plane which is superimposed over the contoured surface and from which z coordinates that represent the distance between the x, y coordinates and the reference plane, can be determined.
Figure 3A is a fragmentary, illustrative view of a section of the corrected replica illustrating the manner of determination of the z components of the contoured surface.
Figure 4 is an exploded, generally perspective view of one form of injection mold constructed in accordance with the method of the invention.
Figure 5 is a generally perspective view of the orthotic shown in Figure 1, the contoured surface of which is spaced apart from a reference plane which is superimposed over the contoured surface and from which z coordinates that represent the distance between the x, y coordinates and the reference plane, can be determined.
Figure 6 is a generally perspective view of a foot impression of the character received from the examining doctor, the contoured surface of which is spaced apart from a reference plane which is superimposed over the contoured surface thereof and from which z coordinates that represent the distance between the x, y coordinates and the reference plane, can be determined.
Discussion of the Invention
[0033] Referring to the drawings and particularly to Figure 1, one form of the functional orthotic produced in accordance with the method of the invention is there shown and generally designated by the numeral 14. The three-dimensional, curved supporting surface 16 of the functional orthotic 14 includes the heel region 18 properly contoured to support the users heel, the arch region 20 contoured to properly support the users arch and the metatarsal region 22 disposed proximate the heads of the users metatarsal joints.
[0034] As previously discussed, functional orthotics of the type generally illustrated in Figure 1 are typically produced in accordance with a relatively standard prior art procedure. The first step in this procedure involves the examination of the patient by the doctor and the forming by the doctor of a negative cast of the patient's foot using plaster of paris, crushable foam, or the like (see, for example, Figure 6). This negative cast is then forwarded to an orthotic laboratory, along with any special instructions the doctor may have concerning the construction of the orthotic for the patient.
[0035] At the orthotic laboratory the negative cast is used to make a plaster of paris positive, or uncorrected replica of the patient's foot. The uncorrected replica is then modified by the laboratory in accordance with the doctor's instructions to produce a corrected replica (see, for example, Figure 3). As previously discussed, the corrections made to the uncorrected replica may include wedging the heel portion by the addition of a plaster platform to simulate the foot in the neutral position. Additionally, the wedged replica may then be further modified with strategically placed plaster of paris buildups to account for fat pad expansion around the heel and along the lateral foot border to allow for compression of the medial arch and transverse arch and to create a smooth transition from the foot platform to the arch and mid-foot.
[0036] After the corrected replica is finished to the satisfaction of the laboratory technical staff, a thermoplastic material, such as polypropylene, is heat molded to the plantar surface of the corrected replica. Finally, the formed thermoplastic material is appropriately trimmed and polished to produce the finished functional orthotic having the general physical characteristics of the orthotic illustrated in Figure 1.
[0037] It has long been recognized that the prior art processes of the character described in the preceding paragraphs are somewhat inefficient and highly labor intensive. For this reason, the present inventor began an exhaustive study to attempt to develop an improved and less costly method of making functional orthotics. In this connection, it has always been assumed that each human foot, like a snowflake, is unique, and that each functional orthotic made for a particular patient is similarly unique. With this in mind, the present inventor set out to verify or refute this long-standing belief by carefully analyzing large numbers of human foot impressions provided by the examining doctor and the uncorrected replicas that had been made in the laboratory from these impressions. Next, the inventor studied the corrected replicas that had been produced from the uncorrected replicas and finally, analyzed the functional orthotics that had been made from the corrected replicas. These studies, the details of which will be discussed in the paragraphs which follow, surprisingly revealed that, in actuality, the functional orthotics produced by the prior art process were not individually unique, but rather, could be grouped into families of substantially identical orthotics. More particularly, the present inventor discovered that although there were subtle differences among the three dimensional surfaces exhibited by the finished orthotics, the orthotics could nevertheless be justifiably grouped into some 540 basic configurations and rarely would a selected one of these basic orthotic configurations not be suitable for corrective use by a particular patient. In fact, the study indicates that from these 540 basic configurations, on the order of 60 configurations can produce about 75 percent of the orthotics made by the laboratory on any given day.
[0038] Turning to Figures 2 through 4, one form of the method of the invention for making injection molds suitable for use in injection molding finished orthotics of the general type shown in Figure 1 is there illustrated. Figure 2 shows a corrected replica made from an uncorrected replica, which, in turn, was made from a foot impression provided by the examining doctor. For example, the first step of one form of the method of the invention for making the injection molds and the finished orthotics involves the selection of a multiplicity of uncorrected replicas of the human foot which have been made from the negative casts or impressions received by the laboratory. It is to be understood that many thousands of casts, replicas and orthotics are in fact analyzed in the accomplishment of the method of the invention.
[0039] Following selection for study of the casts 24, the uncorrected replicas 26 made therefrom and the corrected replicas 28 formed from the uncorrected replicas, the next step in the method of the invention involves identifying the multiplicity of functional orthotics 14, produced from the corrected replicas, which corrected replicas were made by conventional techniques from the multiplicity of corrected replicas 28. Next, the functional orthotics are carefully examined to identify those which exhibit substantially identical contoured upper, or foot engaging surfaces. This done, a plurality of first subgroups is identified by selecting from the multiplicity of functional orthotics those finished orthotics which are of substantially identical configuration.
[0040] Once subgroups are identified, the final step in one form of the method of the invention for making the injection molds comprises the step of constructing for each of said plurality of subgroups an injection mold 30. As shown in Figure 4, the several injection molds constructed in accordance with the methods of the invention each have an internal cavity 30a (Figure 4), which, when filled with a moldable plastic, will produce a finished orthotic having a contoured upper or foot engaging surface which is substantially identical to the contoured upper surfaces of the functional orthotics that make up each of the subgroups, which upper surfaces are formed by pressing a heated thermoplastic blank against a correct replica in the manner previously described herein.
[0041] Once the x, y, z data for either the low contoured surface of the corrected replica or the x, y, z data for the upper foot engaging contoured surface of the orthotic for each subgroup is known, the x, y, z data for the bottom shoe engaging surface of the orthotic can similarly be determined by methods well known to those skilled in the art such as by calculation or by using the same measurement techniques previously described for determining the x, y, z data for the contoured surface. Having the x, y, z data for both the upper and lower surfaces of the orthotic, it is a simple matter to construct the injection mold 30 by techniques well understood by to those skilled in the injection molding art.
[0042] The methods of the invention for making finished functional orthotics for particular patients using the injection molds thus developed obviously involves many of the same steps involved in the methods of the invention for making the injection molds. However, these methods include additional analysis of the information derived during mold development and also include the further important step of generating from the information derived sets of comparison data which can be recorded in comparison tables of x, y, z comparison data. Referring particularly to Figures 1 through 4, developing this important comparison data generally comprises the steps of determining for each of the orthotic subgroups the shape of the contoured surfaces of the foot impressions and uncorrected replicas which were used to construct the corrected replicas which, in turn, were used to form the orthotics that make up each of the orthotic subgroups. Then, after determining the shape of the shoe engaging surface of the particular patient for which the orthotic is to be constructed, this shape can be compared with the sets of comparison data developed to determine which subgroups of foot impressions and uncorrected replicas exhibit contoured surfaces that correspond most closely to the shape of the patients foot. This done, the orthotics formed from the corrected replicas made from the identified uncorrected replicas can be identified. Then it is an easy matter to select the correct mold to be used, which, of course, is the mold that will produce the orthotics thus identified.
[0043] The derivation of the plurality of sets of comparison data necessary to construct an injection molded orthotic based on data derived from the examining doctor can be accomplished in several ways. For example, the x, y, z data for the foot impressions which make up each subgroup that corresponds to orthotic subgroups can first be determined in the manner illustrated in Figure 6 of the drawings. Alternatively, the same x, y, z data can be developed in substantially the same manner through analysis of the uncorrected replicas which make up each subgroup that corresponds to the orthotic subgroups.
[0044] Still another approach to the development of the comparison sets of x, y, z data involves the careful analysis of x, y, z data of the corrected replicas which were made from the uncorrected replicas selected for the study. More particularly, as depicted in Figure 2, in this particular form of the invention, the lower contoured surface of each of the multiplicity of corrected replicas constructed by the laboratory is analyzed in terms of a multiplicity of x, y coordinates of the general character shown by way of example in Figure 2. It is to be understood that in actual practice, many more x, y coordinates than those shown in the drawings were identified on the contoured surface of the corrected replicas. However, for sake of clarity of explanation, only a few such coordinates are shown in the drawings. For example, in the actual mapping of the contoured surfaces, of the finished orthotics, the foot impressions, and the corrected replicas, the x or latitude lines are preferably spaced apart by a distance about 1.0 and 1.4 millimeters and the y, or longitude lines, are preferably spaced apart by a distance of between about 0.5 and 0.7 millimeters (see Figures 3 and 6).
[0045] After the x, y coordinates are defined, the foot impressions 24, uncorrected replica 26, or the finished orthotic 14, as the case may be, is positioned at a spaced-apart location from a reference plane "P" which is typically perpendicular to the bisection of the calcaneus in the manner depicted in Figures 3, 5 and 6. This done, the previously discussed z coordinates are determined. The z coordinates represent the distance between the reference plane "P" and each of the multiplicity of points on the contoured surface which are defined by the intersection of the coordinate x, y lines (see also Figure 3A). The z coordinates can be identified in a number of ways well known to those skilled in the art. For example, conventional inspection techniques using surface plates and dial gages can be used. Additionally, impression units such as described in the previously mentioned prior art patent to Rolloff et al, No. 4,876,758 can be used in conjunction with a suitable computer and computer software to produce digital signals representative of the contoured surface under consideration. Similarly, the contoured surfaces can be scanned directly using computer assisted scanning devices such as, for example, a laser digitizer of a character which is readily commercially available from sources such as Cyberware Company of Pacific Grove, California.
[0046] Considering particularly the method of the invention which involves the mapping of the contoured surface of the multiplicity of corrected replicas, particular reference should be made to Figures 2, 3, and 3A. Corrected replicas are constructed from the multiplicity of uncorrected replicas, which, in turn were formed from impressions. As was the case in accomplishing the method of the invention for making the injection molds, the multiplicity of corrected replicas are first divided into subgroups wherein each corrected replica of a particular subgroup exhibits a substantially identical lower contoured surface.
[0047] Once the corrected replica or second subgroups are thus identified, it is then possible to identify a plurality of third subgroups by identifying for each third subgroup the uncorrected replicas which were corrected to form the corrected replicas which make up the second subgroup.
[0048] Using the x, y, z data derived in the manner discussed in the preceding paragraphs, the comparison tables of the invention can readily be developed. As previously discussed, these important comparison tables are used to select a particular mold 30 for a particular patient based upon the particular shape of the lower shoe engaging surface of the patient's foot. In actually formulating the comparison tables, the x, y, z data previously developed for each of the multiplicity of corrected replicas or finished orthotics is analyzed and correlated with the appropriate uncorrected replica subgroup.
[0049] For each of the sets of corrected replica comparison x, y, z data thus developed, the mold 30 which is associated with that set is identified. For example
[0050] With the foregoing analysis in mind, in carrying out one form of the method of the invention, for making a finished orthotic, when the prescription for a particular patient is received from the examining doctor, the correct mold for producing the orthotic for the new patient can be quickly identified in the following manner. First, from the prescription data received, which may include an impression of the patient's foot, the x, y, z data for contoured lower surface of the patient's foot is determined in the manner illustrated in Figure 6. This patient's x, y, z data is then compared with the groups of x, y, z data found in the comparison table to identify the particular group within which the patient x, y, z data falls. Once this is done, the injection mold which corresponds to the selected comparison group of x, y, z data is identified, and, using the selected injection mold, the finished orthotic for the patient is then injection molded.
[0051] It is to be understood that, as previously discussed, the patient x, y, z data can be determined in a number of ways. For example, as indicated in Figure 6, physical measurements of the impression received from the examining doctor can be used to identify the contour of the shoe engaging portion of the patient's foot. In accordance with this method, x, y coordinates are first identified on the surface of the cavity 24a of the impression (Figure 6). This done, the z coordinates, which are the distances between a reference plane "P" spaced apart from cavity 24a and the points defined by the intersection of the x-y lines, are determined. These z coordinates can be determined in a number of ways well known in the art such as, for example, through use of a depth gage, by electronic scanning or by using mechanical impression units of the general type described in U.S. Patent 4,876,758. After this x, y, z data is obtained and recorded, it can be correlated with the uncorrected and corrected replicas which evolve from the impressions and, finally with the first subgroups of orthotics produced from the corrected replicas. The multiplicity of sets of comparison data which make up the comparison tables can then be derived in the manner previously discussed and then used to select the correct injection mold for molding a finished orthotic for a given patient from which the patient x, y, z data has been determined.
[0052] Alternatively, the equipment and techniques described in U.S. Patent No. 4,876,758 issued to Rolloff et al can be used to measure the mold cavity. Further, mechanical or electronic scanning of the uncorrected replicas made from the foot impressions can be accomplished, or the patient's feet themselves can be analyzed by techniques well known to those skilled in the art to determine the foot contour. In any event, once the patient x, y, z data is derived by any one of the aforementioned methods, it can quickly be compared with the comparison data tables and the proper mold 30 selected from the multiplicity of some five hundred and forty or more molds which have been constructed, identified and cataloged in accordance with the previously described methods of the invention.
[0053] Having now described the invention in detail in accordance with the requirements of the patent statutes, those skilled in this art will have no difficulty in making changes and modifications in the individual parts or their relative assembly in order to meet specific requirements or conditions. Such changes and modifications may be made without departing from the scope of the invention, as set forth in the following claims.
(a) obtaining a multiplicity of corrected replicas (28) of the human foot, each having been made from an uncorrected replica (26) of a different human foot having an uncorrected contoured lower surface, each said corrected replica (28) exhibiting a corrected contoured lower surface from which an orthotic (14) can be formed by heating and pressing a thermoplastic blank thereagainst;
(b) examining each said corrected replica (28) of said selected multiplicity of corrected replicas (28) to map the contoured lower surfaces of the corrected replicas (28), said examination of the corrected replicas (28) is performed by mapping x-, y-, and z-coordinates, inspecting the surface, using a computer and computer software to produce a digital representative of the contoured surface and/or using a computer assisted scanning device;
(c) identifying a plurality of corrected replica subgroups by grouping said multiplicity of corrected replicas (28) which were examined into subgroups in which said corrected replicas (28) which make up each said subgroup exhibit substantially identical contoured lower surfaces; and
(d) constructing for each of said plurality ofsubgroups an injection mold (30) having an internal cavity (30a) which, when filled with a moldable plastic, will produce a finished orthotic (14) having a contoured upper surface substantially identical to the contoured lower surfaces of said corrected replicas (28) which make up each said subgroup.
(a) identifying on the contoured lower surface of each said selected corrected replica a multiplicity of x, y coordinates;
(b) for each said selected corrected replica, defining a plane spanning said contoured lower surface thereof and spaced apart therefrom; and
(c) for each said selected corrected replica, deter-mining and recording for each x, y coordinate identified thereon the distance between the coordinate and said plane, whereby for each said injection mold constructed, a set of x, y, z data can be assigned thereto, said set of x, y, z data defining the contour of the lower surface of the corrected replicas which make up the corrected replica subgroup for which the mold was constructed.
(a) said x coordinates are identified on the said lower surface of each said selected corrected replica in a manner such that each said x coordinate is spaced from the adjacent x coordinate by a distance of between about 1.0 and about 1.4 millimeters; and
(b) said y coordinates are identified on said lower surface of each said selected corrected replica in a manner such that each said y coordinate is spaced from the adjacent y coordinate by a distance of between about 0.5 millimeters and about 0.9 millimeters.
(a) identifying on the contoured lower surface thereof a multiplicity of x, y coordinates;
(b) for each said selected uncorrected replica, defining a plane spanning said contoured lower surface thereof and spaced apart therefrom; and
(c) for each said selected uncorrected replica, determining and recording for each x, y coordinate identified thereon the distance between the coordinate and said plane.
(a) identifying thereon a multiplicity ofx, y coordinates;
(b) for each said selected foot impression defining a base plane spanning said foot impression and being spaced apart therefrom; and
(c) for each said selected foot impression, determining and recording for each x, y coordinate identified thereon the distance between the coordinate and the base plane.
(a) obtaining a multiplicity of orthotics (14) made from a multiplicity of corrected replicas (28), said corrected replicas (28) having been made from different uncorrected replicas (26) having a lower contoured surface substantially replicating the shoe-engaging surface of the human foot;
(b) examining each said orthotic (14) of said multiplicity of selected orthotics to map the contoured upper surfaces of the orthotics, said examination of the orthotics (14) is performed by mapping x-, y-, and z-coordinates, inspecting the surface, using a computer and computer software to produce a digital representative of the contoured surface and/or using a computer assisted scanning device;
(c) identifying a plurality of orthotic subgroups by dividing said orthotics (14) examined into subgroups in which said finished orthotics (14) which make up each said subgroup exhibit substantially identical, contoured upper surfaces; and
(d) constructing for each of said plurality ofsubgroups an injection mold (30) having an internal cavity (30a) which, when filled with a moldable plastic, will produce a finished orthotic (14) having a contoured upper surface substantially identical to the contoured upper surface of said orthotics (14) which make up each subgroup.
(a) identifying on the contoured upper surface of each said selected functional orthotic a multiplicity of x, y coordinates;
(b) for each said selected functional orthotic defining a plane spanning said contoured upper surface thereof and spaced apart therefrom; and
(c) for each said selected functional orthotic determining and recording for each x, y coordinate identified thereon the distance between the coordinate and said plane, whereby for each said injection mold made, a set of x, y, z data can be assigned thereto, said set of x, y, z data defining the contour ofthe upper surface of the functional orthotics which make up the functional orthotic subgroup for which the mold was constructed.
(a) identifying on the contoured lower surface thereof a multiplicity of x, y coordinates;
(b) for each said selected corrected replica, defining a plane spanning said contoured lower surface thereof and spaced apart therefrom; and
(c) for each said selected corrected replica, deter mining and recording for each x, y coordinate identified thereon the distance between the coordinate and said plane.
(a) identifying on the contoured lower surface thereof a multiplicity of x, y coordinates;
(b) for each said selected uncorrected replica, defining a plane spanning said contoured lower surface thereof and spaced apart therefrom; and
(c) for each said selected uncorrected replica, determining and recording for each x, y coordinate identified thereon the distance between the coordinate and said plane.
(a) identifying thereon a multiplicity ofx, y coordinates;
(b) for each said selected foot impression defining a base plane spanning said foot impression and being spaced apart therefrom; and
(c) for each said selected foot impression, determining and recording for each x, y coordinate identified thereon the distance between the coordinate and the base plane.
(i) selecting a multiplicity of uncorrected replicas of the human foot, each having an uncorrected contoured lower surface and each of which is later to be corrected to form a corrected replica having a corrected contoured surface from which an orthotic can be made;
(ii) identifying a multiplicity of corrected replicas made from said multiplicity of uncorrected replicas; and
(iii) identifying the multiplicity of orthotics made from said multiplicity of corrected replicas.
(a) identifying a plurality of second subgroups by dividing said multiplicity of corrected replicas into second subgroups in which said corrected replicas which make up each said second subgroup exhibit substantially identical lower contoured surfaces;
(b) identifying a plurality of third subgroups by identifying for each said second subgroup the uncorrected replicas which were corrected to form said corrected replicas which make up said second subgroup;
(c) for each said uncorrected replica of each of said plurality of third subgroups:
(i) identifying on the contoured lower surface thereof a multiplicity of x, y coordinates;
(ii) defining a plane spanning said contoured lower surface and spaced apart therefrom; and
(iii) determining and recording for each x, y coordinate identified on each said uncorrected replica of said third subgroups the distance between the coordinate and said plane.
(a) identifying thereon a multiplicity of x, y coordinates;
(b) for each said selected individual foot impression, defining a base plane spanning said contoured surface and spaced apart therefrom; and
(c) for each said selected individual foot impression determining and recording for each y, y coordinate identified on each said selected individual foot impression the distance between the coordinate and the base plane.
(i) selecting a multiplicity of impressions of the human foot, each having a cavity having a contoured surface which cavity is later to be used to form an uncorrected replica which, in turn, is later to be corrected to form a corrected replica having a corrected contoured surface from which an orthotic can be formed; and
(ii) identifying the functional orthotics made from said corrected replicas.
(a) identifying a plurality of second subgroups by dividing the corrected replicas into second subgroups in which said corrected replicas which make up each said second subgroup exhibit substantially identical lower contoured surfaces;
(b) identifying a plurality of third subgroups by identifying for each said second subgroup the uncorrected replicas which were corrected to form said corrected replicas which make up said second subgroup;
(c) identifying a plurality of subgroups of foot impressions by identifying for each subgroup the foot impressions used to form said uncorrected replicas which make up said third subgroup;
(d) for each said foot impression of each of said plurality of foot impression subgroups:
(i) identifying on the contoured surface of the cavity thereof a multiplicity of x, y coordinates;
(ii) defining a plane spanning said contoured surface and spaced apart therefrom; and
(iii) determining and recording for each x, y coordinate identified on said contoured surface the distance between the coordinate and said plane,
(e) formulating a plurality of sets of comparison data by determining for each of said orthotic subgroups the shape of the contour of the contoured surfaces of the foot impressions and uncorrected replicas which were used to construct the corrected replicas which, in turn, were used to form the orthotics which make up each of said orthotic subgroups;
(f) determining the shape of the contour of the shoe engaging surface of the patient's foot;
(g) comparing said shape of the contour of the shoe engaging surface of the patient's foot thus determined with said sets of comparison data to identify the particular set of comparison data that defines the shape of the contoured surfaces of said foot impression and uncorrected replicas that most nearly correspond to said shape of the contour ofthe shoe-engaging surface of the patient's foot;
(h) identifying said orthotic subgroup which consists of orthotics formed from the corrected replicas made from the uncorrected replicas which exhibit a contoured surface shape that corresponds to the shapes defined in the identified set of comparison data;
(i) selecting the injection mold constructed for said identified orthotic subgroup; and
(j) molding from said selected mold a finished orthotic for the patient.
(a)identifying on said contoured surface a multiplicity of x, y coordinates;
(b) defining a base plane spanning said foot impression and being spaced apart therefrom; and
(c) determining and recording for each x, y coordinate identified thereon the distance between the coordinate and the base plane.
(a) identifying on said contoured surface a multiplicity of x, y coordinates;
(b) defining a base plane spanning said contoured surface of said uncorrected replica and being spaced apart therefrom; and
(c) determining and recording for each x, y coordinate identified thereon the distance between the coordinate and the base plane.
(a) selecting a multiplicity of corrected replicas (28) of the human foot, each having been made from an uncorrected replica (26) of a different human foot having an uncorrected contoured lower surface, each said corrected replica (28) exhibiting a corrected contoured lower surface from which an orthotic (14) could be formed by heating and pressing a thermoplastic blank thereagainst;
(b) examining each said corrected replica (28) of said selected multiplicity of corrected replicas to identify those having substantially identical contoured lower surfaces;
(c) identifying a plurality of corrected replica subgroups by grouping said multiplicity of corrected replicas (28) which were examined into subgroups in which said corrected replicas (28) which make up each said subgroup exhibit substantially identical contoured lower surfaces;
(d) constructing for each of said plurality of subgroups an injection mold (30) having an internal cavity (30a) which, when filled with a moldable plastic, will produce a finished orthotic (14) having a contoured upper surface substantially identical to the contoured lower surfaces of said corrected replicas (28) which make up each said subgroup;
(e) formulating a plurality of sets of comparison data by determining for each of said corrected replica subgroups the shape of the contour of the contoured surfaces of the foot impressions and uncorrected replicas (26) which were used to construct the corrected replicas (28) which make up each of said corrected replica subgroups;
(f) determining the contour of the shoe-engaging surface of the patient's foot;
(g) comparing said contour of the shoe-engaging surface of the patient's foot thus determined with said sets of comparison data to identify the particular set of comparison data that defines the shape of the contoured surfaces of said foot impression and uncorrected replicas (28) that most nearly corresponds to said shape of the contour ofthe shoe engaging surface of the patient's foot;
(h) identifying the corrected replica subgroup which consists of corrected replicas (28) constructed using the uncorrected replicas (26) which exhibit a contoured surface shape that corresponds to the shapes defined in the identified set of comparison data;
(i) selecting said injection mold (30) constructed for said identified corrected replica subgroup; and
(ii) (j) molding from said selected mold (30) a finished orthotic (14) for the patient.
(a) identifying on said contoured surface a multiplicity of x, y coordinates;
(b) defining a base plane spanning said foot impression and being spaced apart therefrom; and
(c) determining and recording for each x, y coordinate identified thereon the distance between the coordinate and the base plane.
(a) identifying on said contoured surface a multiplicity of x, y coordinates;
(b) defining a base plane spanning said contoured surface of said uncorrected replica and being spaced apart therefrom; and
(c) determining and recording for each x, y coordinate identified thereon the distance between the coordinate and the base plane.
(a) selecting a multiplicity of different replicas of the human foot, each of which is later to be used to form by conventional techniques a corrected replica (28) having a corrected contoured surface from which an orthotic (14) can be formed;
(b) selecting a multiplicity of corrected replicas (28) from those made from said multiplicity of selected replicas of the human foot;
(c) selecting a multiplicity of functional orthotics (14) from those made from said multiplicity of selected corrected replicas (28);
(d) identifying a plurality of first subgroups by examining each said functional orthotic (14) of said multiplicity of functional orthotics selected to identify those functional orthotics having a substantially identical contoured upper surface;
(e) producing a multiplicity ofinjection molds (30) by constructing for each of said plurality of first subgroups an injection mold (30) having an internal cavity (30a) which, when filled with a moldable plastic, will produce a finished orthotic (14) having a contoured upper surface substantially identical to the contoured upper surface of said functional orthotics (14) which make up each said subgroup;
(f) identifying a plurality of second subgroups by dividing said multiplicity of corrected replicas (28) selected into second subgroups in which said corrected replicas (28) which make up such said second subgroup exhibit substantially identical lower contoured surfaces;
(g) identifying a plurality of third subgroups by identifying for each said second subgroup the uncorrected replicas (26) which were corrected to form said corrected replicas (28) which make up said second subgroup;
(h) producing a first set of comparison data by analyzing said plurality ofsaid third subgroups of uncorrected replicas (26) and for each said uncorrected replica (26) of each of said plurality of said third subgroups:
(i) identifying on the contoured lower surface thereof a multiplicity of x, y coordinates;
(ii) defining a reference plane spanning said contoured lower surface and spaced apart therefrom;
(iii) determining and recording for each x, y coordinate identified on each said uncorrected replica (26) of said third subgroups the distance between the coordinate and said reference plane;
(i) determining and recording x, y, z data for the contoured lower surface of the patient's foot by determining, for each of a multiplicity of x, y coordinates defined on said contoured lower surface thereof, the height of the coordinate above a reference plane to develop patient x, y, z data;
(j) comparing said patient x, y, z data with said comparison groups of x, y, z data to identify the comparison group of x, y, z data within which said patient x, y, z data falls;
(k) selecting said injection mold (30) which corresponds to said selected comparison group of x, y, z data; and
(l) molding from said selected injection mold (30) the finished orthotic (14).
a) Gewinnung einer Vielzahl von korrigierten Nachbildungen (28) des menschlichen Fusses, deren jede von einer unkorrigierten Nachbildung (26) eines unterschiedlichen menschlichen Fusses mit einer unkorrigierten profilierten Unterseite hergestellt wurde, wobei jede korrigierte Nachbildung (28) eine korrigierte profilierte Unterseite aufweist, von der eine Orthese (14) durch Erhitzen und Andrücken eines thermoplastischen Rohlings abgeformt werden kann;
b) Untersuchung jeder korrigierten Nachbildung (28) aus der ausgewählten Vielzahl von korrigierten Nachbildungen (28), um die profilierten Unterseiten der korrigierten Nachbildungen (28) abzubilden, wobei diese Untersuchung der korrigierten Nachbildungen (28) durch Abbildung von x-, y- und z-Koordinaten, Prüfung der Oberfläche, Verwendung eines Computers und von Computersoftware zur Herstellung eines digitalen Vertreters der profilierten Oberfläche und/oder Verwendung eines rechnergestützten Scanners ausgeführt wird;
c) Identifizierung einer Mehrzahl von Untergruppen korrigierter Nachbildungen durch Gruppierung der Vielzahl untersuchter korrigierter Nachbildungen (28) zu Untergruppen, in denen die jede Untergruppe bildenden, korrigierten Nachbildungen (28) im Wesentlichen identische profilierte Unterseiten aufweisen; und
d) für jede der Mehrzahl von Untergruppen Konstruktion einer Spritzform (30) mit einem inneren Hohlraum (30a), der nach Füllung mit einem spritzfähigen Kunststoff eine fertige Orthese (14) liefert, die eine profilierte Oberseite besitzt, die im Wesentlichen mit den profilierten Unterseiten der korrigierten Nachbildungen (28) identisch ist, aus denen jede Untergruppe besteht.
a) Identifizierung einer Vielzahl von x, y-Koordinaten auf der profilierten Unterseite jeder ausgewählten korrigierten Nachbildung;
b) für jede ausgewählte korrigierte Nachbildung Definition einer Ebene, die deren profilierte Unterseite überspannt und davon beabstandet ist; und
c) für jede ausgewählte korrigierte Nachbildung und jede darauf identifizierte x,y-Koordinate Bestimmung und Aufzeichnung des Abstandes zwischen der Koordinate und der Ebene, wodurch jeder konstruierten Spritzform ein Satz von x,y,z-Daten zugeordnet werden kann, wobei dieser Satz von x,y,z-Daten die Konturen der Unterseite der korrigierten Nachbildungen definiert, aus denen die Untergruppe korrigierter Nachbildungen besteht, für die die Spritzform konstruiert worden war.
a) die x-Koordinaten auf der Unterseite jeder ausgewählten korrigierten Nachbildung derart identifiziert werden, dass jede x-Koordinate von der benachbarten x-Koordinate durch einen Abstand zwischen etwa 1,0 und etwa 1,4 Millimetern getrennt ist; und
b) die y-Koordinaten auf der Unterseite jeder ausgewählten korrigierten Nachbildung derart identifiziert werden, dass jede y-Koordinate von der benachbarten y-Koordinate durch einen Abstand zwischen etwa 0,5 Millimetern und etwa 0,9 Millimetern getrennt ist.
a) auf deren profilierter Unterseite eine Vielzahl von x,y-Koordinaten zu identifizieren;
b) für jede ausgewählte unkorrigierte Nachbildung eine Ebene zu definieren, die deren profilierte Unterseite überspannt und davon beabstandet ist; und
c) für jede ausgewählte unkorrigierte Nachbildung und jede darauf identifizierte x,y-Koordinate den Abstand zwischen der Koordinate und der Ebene zu bestimmen und aufzuzeichnen.
a) eine Vielzahl von x,y-Koordinaten darauf zu identifizieren;
b) für jeden ausgewählten Fussabdruck eine Basisebene zu definieren, die den Fussabdruck überspannt und davon beabstandet ist; und
c) für jeden ausgewählten Fussabdruck und jede darauf identifizierte x,y-Koordinate den Abstand zwischen der Koordinate und der Basisebene zu bestimmen und aufzuzeichnen.
a) Gewinnung einer Vielzahl von Orthesen (14), die aus einer Vielzahl von korrigierten Nachbildungen (28) hergestellt worden sind, wobei die korrigierten Nachbildungen (28) von unterschiedlichen unkorrigierten Nachbildungen (26) hergestellt worden waren, die eine profilierte Unterseite besitzen, die im Wesentlichen die am Schuh Halt findende Oberfläche des menschlichen Fusses nachbildet;
b) Untersuchung jeder Orthese (14) aus der Vielzahl von ausgewählten Orthesen, um die profilierten Oberseiten der Orthesen abzubilden, wobei diese Untersuchung der Orthesen (14) durch Abbildung von x-, y- und z-Koordinaten, Prüfung der Oberfläche, Verwendung eines Computers und von Computersoftware zur Herstellung eines digitalen Vertreters der profilierten Oberfläche und/oder Verwendung eines rechnergestützten Scanners ausgeführt wird;
c) Identifizierung einer Mehrzahl von Untergruppen von Orthesen durch Unterteilung der untersuchten Orthesen (14) in Untergruppen, in denen die fertigen Orthesen (14), die jede Untergruppe bilden, im Wesentlichen identische profilierte Oberseiten aufweisen; und
d) für jede aus der Mehrzahl von Untergruppen Konstruktion einer Spritzform (30) mit einem inneren Hohlraum (30a), der nach Füllung mit einem spritzfähigen Kunststoff eine fertige Orthese (14) liefert, die eine profilierte Oberseite besitzt, die im Wesentlichen mit der profilierten Oberseite der Orthesen (14) identisch ist, aus denen jede Untergruppe besteht.
a) Identifizierung einer Vielzahl von x, y-Koordinaten auf der profilierten Oberseite jeder ausgewählten funktionellen Orthese;
b) für jede ausgewählte funktionelle Orthese Definition einer Ebene, die deren profilierte Oberseite überspannt und davon beabstandet ist; und
c) für jede ausgewählte funktionelle Orthese und jede darauf identifizierte x,y-Koordinate Bestimmung und Aufzeichnung des Abstandes zwischen der Koordinate und der Ebene, wodurch jeder hergestellten Spritzform ein Satz von x,y,z-Daten zugeordnet werden kann, wobei dieser Satz von x,y,z-Daten die Konturen der Oberseite der funktionellen Orthesen definiert, die die Untergruppe funktioneller Orthesen bilden, für die die Spritzform konstruiert worden war.
a) auf deren profilierter Unterseite eine Vielzahl von x,y-Koordinaten zu identifizieren;
b) für jede ausgewählte korrigierte Nachbildung eine Ebene zu definieren, die deren profilierte Unterseite überspannt und davon beabstandet ist; und
c) für jede ausgewählte korrigierte Nachbildung und jede darauf identifizierte x,y-Koordinate den Abstand zwischen der Koordinate und der Ebene zu bestimmen und aufzuzeichnen.
a) auf deren profilierter Unterseite eine Vielzahl von x,y-Koordinaten zu identifizieren;
b) für jede ausgewählte unkorrigierte Nachbildung eine Ebene zu definieren, die deren profilierte Unterseite überspannt und davon beabstandet ist; und
c) für jede ausgewählte unkorrigierte Nachbildung und jede darauf identifizierte x,y-Koordinate den Abstand zwischen der Koordinate und der Ebene zu bestimmen und aufzuzeichnen.
a) eine Vielzahl von x,y-Koordinaten darauf zu identifizieren;
b) für jeden ausgewählten Fussabdruck eine Basisebene zu definieren, die den Fussabdruck überspannt und davon beabstandet ist; und
c) für jeden ausgewählten Fussabdruck und jede darauf identifizierte x,y-Koordinate den Abstand zwischen der Koordinate und der Basisebene zu bestimmen und aufzuzeichnen.
I) Auswahl einer Vielzahl unkorrigierter Nachbildungen des menschlichen Fusses, deren jede eine unkorrigierte profilierte Unterseite aufweist und später zu korrigieren ist, um eine korrigierte Nachbildung zu bilden, die eine korrigierte profilierte Oberfläche besitzt, von der eine Orthese hergestellt werden kann;
II) Identifizierung einer Vielzahl von korrigierten Nachbildungen, die aus der Vielzahl unkorrigierter Nachbildungen hergestellt worden sind; und
III) Identifizierung der Vielzahl von Orthesen, die aus der Vielzahl korrigierter Nachbildungen hergestellt worden sind.
a) Identifizierung einer Mehrzahl zweiter Untergruppen, indem die Vielzahl korrigierter Nachbildungen in zweite Untergruppen unterteilt wird, in denen die korrigierten Nachbildungen, aus denen jede der zweiten Untergruppen besteht, im Wesentlichen identische profilierte Unterseiten aufweisen;
b) Identifizierung einer Mehrzahl dritter Untergruppen, indem für jede der zweiten Untergruppen die unkorrigierten Nachbildungen identifiziert werden, die korrigiert worden waren, um die korrigierten Nachbildungen zu bilden, aus denen die zweite Untergruppe besteht;
c) für jede unkorrigierte Nachbildung jeder der Mehrzahl von dritten Untergruppen:
I) Identifizierung einer Vielzahl von x,y-Koordinaten auf deren profilierter Unterseite;
II) Definition einer Ebene, die die profilierte Unterseite überspannt und davon beabstandet ist; und
III) Bestimmung und Aufzeichnung des Abstandes zwischen der Koordinate und der Ebene für jede der auf jeder unkorrigierten Nachbildung der dritten Untergruppen identifizierten x,y-Koordinaten.
a) eine Vielzahl von x,y-Koordinaten darauf zu identifizieren;
b) für jeden ausgewählten individuellen Fussabdruck eine Basisebene zu definieren, die die profilierte Oberfläche überspannt and davon beabstandet ist; und
c) für jeden ausgewählten individuellen Fussabdruck und jede auf jedem ausgewählten individuellen Fussabdruck identifizierte y,y-Koordinate den Abstand zwischen der Koordinate und der Basisebene zu bestimmen und aufzuzeichnen.
I) Auswahl einer Vielzahl von menschlichen Fussabdrücken, deren jeder einen Hohlraum mit einer profilierten Oberfläche besitzt, der später dafür verwendet wird, eine unkorrigierte Nachbildung zu bilden, die ihrerseits später korrigiert wird, um eine korrigierte Nachbildung zu bilden, die eine korrigierte profilierte Oberfläche besitzt, von der eine Orthese abgeformt werden kann; und
II) Identifizierung der von den korrigierten Nachbildungen hergestellten funktionellen Orthesen.
a) Identifizierung einer Mehrzahl von zweiten Untergruppen, indem die korrigierten Nachbildungen in zweite Untergruppen unterteilt werden, in denen die korrigierten Nachbildungen, aus denen jede der zweiten Untergruppen besteht, im Wesentlichen identische profilierte Unterseiten aufweisen;
b) Identifizierung einer Mehrzahl dritter Untergruppen, indem für jede der zweiten Untergruppen die unkorrigierten Nachbildungen identifiziert werden, die korrigiert worden waren, um die korrigierten Nachbildungen zu bilden, aus denen die zweite Untergruppe besteht;
c) Identifizierung einer Mehrzahl von Untergruppen von Fussabdrücken, indem für jede Untergruppe die Fussabdrücke identifiziert werden, die verwendet worden waren, um die unkorrigierten Nachbildungen zu bilden, aus denen die dritte Untergruppe besteht;
d) für jeden Fussabdruck jeder der Mehrzahl von Fussabdruckuntergruppene
I) Identifizierung einer Vielzahl von x,y-Koordinaten auf der profilierten Oberfläche seines Hohlraumes;
II) Definition einer Ebene, die die profilierte Oberfläche überspannt und davon beabstandet ist; und
III) Bestimmung und Aufzeichnung des Abstandes zwischen der Koordinate und der Ebene für jede auf der profilierten Oberfläche identifizierte x,y-Koordinate.
e) Formulierung einer Mehrzahl von Sätzen von Vergleichsdaten, indem für jede der Untergruppen von Orthesen die Gestalt der Konturen der profilierten Oberflächen der Fussabdrücke und unkorrigierten Nachbildungen bestimmt wird, die benutzt worden war, die korrigierten Nachbildungen zu konstruieren, die ihrerseits verwendet worden sind, um die Orthesen zu formen, aus denen jede der Untergruppen von Orthesen besteht;
f) Bestimmung der Gestalt der Konturen der am Schuh Halt findenden Oberfläche des Fusses des Patienten;
g) Vergleich der so bestimmten Gestalt der Konturen der am Schuh Halt findenden Oberfläche des Fusses des Patienten mit den Sätzen von Vergleichsdaten, um den konkreten Satz von die Gestalt der profilierten Oberflächen des Fussabdrucks und der unkorrigierten Nachbildungen definierenden Vergleichsdaten zu identifizieren, der der Gestalt der Konturen der am Schuh Halt findenden Oberfläche des Fusses des Patienten am besten entspricht;
h) Identifizierung der Untergruppe von Orthesen, die aus Orthesen besteht, die aus den korrigierten Nachbildungen geformt worden sind, die von den unkorrigierten Nachbildungen hergestellt worden waren, die eine profilierte Oberflächengestalt aufweisen, die den Gestalten entspricht, die im identifizierten Satz von Vergleichsdaten definiert werden;
i) Auswahl der Spritzform, die für die identifizierte Untergruppe von Orthesen konstruiert worden ist; und
j) Spritzgiessen einer fertigen Orthese für den Patienten mit der ausgewählten Spritzform.
a) Identifizierung einer Vielzahl von x,y-Koordinaten auf der profilierten Oberfläche;
b) Definition einer Basisebene, die den Fussabdruck überspannt und davon beabstandet ist;
c) Bestimmung und Aufzeichnung des Abstandes zwischen der Koordinate und der Basisebene für jede darauf identifizierte x,y-Koordinate.
a) Identifizierung einer Vielzahl von x,y-Koordinaten auf der profilierten Oberfläche;
b) Definition einer Basisebene, die die profilierte Oberfläche der unkorrigierten Nachbildung überspannt und davon beabstandet ist; und
c) Bestimmung und Aufzeichnung des Abstandes zwischen der Koordinate und der Basisebene für jede darauf identifizierte x,y-Koordinate.
a) Auswahl einer Vielzahl korrigierter Nachbildungen (28) des menschlichen Fusses, deren jede von einer unkorrigierten Nachbildung (26) eines unterschiedlichen menschlichen Fusses hergestellt worden war und eine unkorrigierte profilierte Unterseite besitzt, wobei jede korrigierte Nachbildung (28) eine korrigierte profilierte Unterseite aufweist, von der eine Orthese (14) durch Erhitzen und Andrücken eines thermoplastischen Rohlings abgeformt werden könnte;
b) Untersuchung jeder korrigierten Nachbildung (28) aus der ausgewählten Vielzahl von korrigierten Nachbildungen, um diejenigen zu identifizieren, die im Wesentlichen identische profilierte Unterseiten besitzen;
c) Identifizierung einer Mehrzahl von Untergruppen korrigierter Nachbildungen durch Gruppierung der Vielzahl untersuchter korrigierter Nachbildungen (28) zu Untergruppen, in denen die jede Untergruppe bildenden, korrigierten Nachbildungen (28) im Wesentlichen identische profilierte Unterseiten aufweisen;
d) für jede der Mehrzahl von Untergruppen Konstruktion einer Spritzform (30) mit einem inneren Hohlraum (30a), der nach Füllung mit einem spritzfähigen Kunststoff eine fertige Orthese (14) liefert, die eine profilierte Oberseite besitzt, die im Wesentlichen mit den profilierten Unterseiten der korrigierten Nachbildungen (28) identisch ist, aus denen jede Untergruppe besteht;
e) Formulierung einer Mehrzahl von Sätzen von Vergleichsdaten, indem für jede der Untergruppen von korrigieren Nachbildungen die Gestalt der Konturen der profilierten Oberflächen der Fussabdrücke und der unkorrigierten Nachbildungen (26) bestimmt wird, die benutzt worden war, um die korrigierten Nachbildungen (28) zu konstruieren, aus denen jede der Untergruppen korrigierter Nachbildungen besteht;
f) Bestimmung der Konturen der am Schuh Halt findenden Oberfläche des Fusses des Patienten;
g) Vergleich der so bestimmten Konturen der am Schuh Halt findenden Oberfläche des Fusses des Patienten mit den Sätzen von Vergleichsdaten, um den konkreten Satz von die Gestalt der profilierten Oberflächen des Fussabdrucks und der unkorrigierten Nachbildungen (26) definierenden Vergleichsdaten zu identifizieren, der der Gestalt der Konturen der am Schuh Halt findenden Oberfläche des Fusses des Patienten am besten entspricht;
h) Identifizierung der Untergruppe korrigierter Nachbildungen, die aus den korrigierten Nachbildungen (28) besteht, die unter Verwendung der unkorrigierten Nachbildungen (26) konstruiert worden waren, die eine profilierte Oberflächengestalt aufweisen, die den Gestalten entspricht, die im identifizierten Satz von Vergleichsdaten definiert werden;
i) Auswahl der Spritzform (30), die für die identifizierte Untergruppe korrigierter Nachbildungen konstruiert worden ist; und
j) Spritzgiessen einer fertigen Orthese (14) für den Patienten mit der ausgewählten Spritzform (30).
a) Identifizierung einer Vielzahl von x,y-Koordinaten auf der profilierten Oberfläche;
b) Definition einer Basisebene, die den Fussabdruck überspannt und davon beabstandet ist; und
c) Bestimmung und Aufzeichnung des Abstandes zwischen der Koordinate und der Basisebene für jede darauf identifizierte x,y-Koordinate,
a) Identifizierung einer Vielzahl von x,y-Koordinaten auf der profilierten Oberfläche;
b) Definition einer Basisebene, die die profilierte Oberfläche der unkorrigierten Nachbildung überspannt und davon beabstandet ist; und
c) Bestimmung und Aufzeichnung des Abstandes zwischen der Koordinate und der Basisebene für jede darauf identifizierte x,y-Koordinate.
a) Auswahl einer Vielzahl unterschiedlicher Nachbildungen des menschlichen Fusses, deren jede später verwendet wird, um mit herkömmlichen Techniken eine korrigierte Nachbildung (28) zu formen, die eine korrigierte profilierte Oberfläche besitzt, von der eine Orthese (14) abgeformt werden kann;
b) Auswahl einer Vielzahl korrigierter Nachbildungen (28) unter den mit der Vielzahl ausgewählter Nachbildungen des menschlichen Fusses hergestellten;
c) Auswahl einer Vielzahl funktioneller Orthesen (14) unter den mit der Vielzahl ausgewählter korrigierter Nachbildungen (28) hergestellten;
d) Identifizierung einer Mehrzahl erster Untergruppen durch Untersuchung jeder funktionellen Orthese (14) aus der Vielzahl ausgewählter funktioneller Orthesen, um diejenigen funktionellen Orthesen auszuwählen, die eine im Wesentlichen identische profilierte Oberseite besitzen;
e) Herstellung einer Vielzahl von Spritzformen (30), indem für jede der Mehrzahl erster Untergruppen eine Spritzform (30) konstruiert wird, die einen inneren Hohlraum (30a) besitzt, der nach Füllung mit einem spritzfähigen Kunststoff eine fertige Orthese (14) liefert, die eine profilierte Oberseite besitzt, die im Wesentlichen mit der profilierten Oberseite der funktionellen Orthesen (14) identisch ist, aus denen jede Untergruppe besteht;
f) Identifizierung einer Mehrzahl zweiter Untergruppen durch Unterteilung der Vielzahl von ausgewählten korrigierten Nachbildungen (28) in zweite Untergruppen, in denen die korrigierten Nachbildungen (28), aus denen eine solche zweite Untergruppe besteht, im Wesentlichen identische profilierte Unterseiten aufweisen;
g) Identifizierung einer Mehrzahl dritter Untergruppen, indem für jede der zweiten Untergruppen die unkorrigierten Nachbildungen (26) identifiziert werden, die korrigiert worden waren, um die korrigierten Nachbildungen (28) zu formen, aus denen die zweite Untergruppe besteht;
h) Herstellung eines ersten Satzes von Vergleichsdaten durch Analyse der Mehrzahl dritter Untergruppen unkorrigierter Nachbildungen (26) und, für jede unkorrigierte Nachbildung (26) jeder der Mehrzahl von dritten Untergruppen:
I) Identifizierung einer Vielzahl von x,y-Koordinaten auf deren profilierter Unterseite;
II) Definition einer Bezugsebene, die die profilierte Unterseite überspannt und davon beabstandet ist;
III) Bestimmung und Aufzeichnung des Abstandes zwischen der Koordinate und der Bezugsebene für jede auf jeder unkorrigierten Nachbildung (26) der dritten Untergruppen identifizierte x,y-Koordinate;
i) Bestimmung und Aufzeichnung von x,y,z-Daten für die profilierte Unterseite des Fusses des Patienten durch Bestimmung der Höhe der Koordinate über einer Bezugsebene für jede einer Vielzahl von auf dessen profilierter Unterseite definierten x,y-Koordinaten, um x,y,z-Daten des Patienten zu entwickeln;
j) Vergleich der x,y,z-Daten des Patienten mit den Vergleichsgruppen von x,y,z-Daten, um die Vergleichsgruppe von x,y,z-Daten zu identifizieren, in die die x,y,z-Daten des Patienten fallen;
k) Auswahl der Spritzform (30), die der ausgewählten Vergleichsgruppe von x,y,z-Daten entspricht; und
l) Spritzgiessen der fertigen Orthese (14) mit der ausgewählten Spritzform (30).
(a) obtenir une multiplicité de répliques corrigées (28) du pied humain, chacune ayant été fabriquée à partir d'une réplique non corrigée (26) d'un pied humain différent ayant une surface inférieure façonnée non corrigée, chaque dite réplique corrigée (28) affichant une surface inférieure façonnée corrigée à partir de laquelle une orthèse (14) peut être formée par chauffage et pressage d'une préforme thermoplastique contre celle-ci ;
(b) examiner chaque dite réplique corrigée (28) de ladite multiplicité sélectionnée de répliques corrigées (28) pour représenter graphiquement les surfaces inférieures façonnées des répliques corrigées (28), ledit examen des répliques corrigées (28) est effectué en représentant graphiquement les coordonnées x, y et z, en inspectant la surface, en utilisant un ordinateur et un logiciel informatique pour produire un représentant numérique de la surface façonnée et/ou en utilisant un dispositif de balayage optique assisté par ordinateur ;
(c) identifier une pluralité de sous-groupes de répliques corrigées en groupant ladite multiplicité de répliques corrigées (28) qui ont été examinées en sous-groupes dans lesquels lesdites répliques corrigées (28) qui constituent chaque dit sous-groupe affichent des surfaces inférieures façonnées sensiblement identiques ; et
(d) construire pour chacun de ladite pluralité de sous-groupes un moule à injection (30) ayant une cavité interne (30a) qui, lorsqu'elle est remplie d'un plastique moulable, produira une orthèse finie (14) ayant une surface supérieure façonnée substantiellement identique aux surfaces inférieures façonnées desdites répliques corrigées (28) qui constituent chaque dit sous-groupe.
(a) identifier sur la surface inférieure façonnée de chaque dite réplique corrigée sélectionnée une multiplicité de coordonnées x, y ;
(b) pour chaque dite réplique corrigée sélectionnée, définir un plan couvrant ladite surface inférieure façonnée de celle-ci et espacé de celle-ci ; et
(c) pour chaque dite réplique corrigée sélectionnée, déterminer et enregistrer pour chaque coordonnée x, y identifiée sur celle-ci la distance entre la coordonnée et ledit plan, d'où il résulte que pour chaque dit moule à injection construit, un ensemble de données x, y, z peut être attribué à celui-ci, ledit ensemble de données x, y, z définissant le contour de la surface inférieure des répliques corrigées qui constituent le sous-groupe de répliques corrigées pour lequel le moule a été fabriqué.
(a) lesdites coordonnées x sont identifiées sur ladite surface inférieure de chaque dite réplique corrigée sélectionnée d'une manière telle que chaque dite coordonnée x est espacée de la coordonnée x adjacente d'une distance d'entre environ 1,0 et environ 1,4 millimètre ; et
(b) lesdites coordonnées y sont identifiées sur ladite surface inférieure de chaque dite réplique corrigée sélectionnée d'une manière telle que chaque dite coordonnée y est espacée de la coordonnée y adjacente d'une distance d'entre environ 0,5 millimètre et environ 0,9 millimètre.
(a) identifier sur la surface inférieure façonnée de celle-ci une multiplicité de coordonnées x, y ;
(b) pour chaque dite réplique non corrigée sélectionnée, définir un plan couvrant ladite surface inférieure façonnée de celle-ci et espacé de celle-ci ; et
(c) pour chaque dite réplique non corrigée sélectionnée, déterminer et enregistrer pour chaque coordonnée x, y identifiée sur celle-ci la distance entre la coordonnée et ledit plan.
(a) identifier sur celle-ci une multiplicité de coordonnées x, y ;
(b) pour chaque dite impression de pied sélectionnée, définir un plan couvrant ladite impression de pied et espacé de celle-ci ; et
(c) pour chaque dite impression de pied sélectionnée, déterminer et enregistrer pour chaque coordonnée x, y identifiée sur celle-ci la distance entre la coordonnée et ledit plan.
(a) obtenir une multiplicité d'orthèses (14) fabriquées à partir d'une multiplicité de répliques corrigées (28), lesdites répliques corrigées (28) ayant été fabriquées à partir de répliques non corrigées (26) différentes ayant une surface inférieure façonnée répliquant substantiellement la surface d'engagement dans la chaussure du pied humain ;
(b) examiner chaque dite orthèse (14) de ladite multiplicité d'orthèses sélectionnées pour représenter graphiquement les surfaces supérieures façonnées des orthèses, ledit examen des orthèses (14) est effectué en représentant graphiquement les coordonnées x, y et z, en inspectant la surface, en utilisant un ordinateur et un logiciel informatique pour produire un représentant numérique de la surface façonnée et/ou en utilisant un dispositif de balayage optique assisté par ordinateur ;
(c) identifier une pluralité de sous-groupes d'orthèses en divisant lesdites orthèses (14) examinées en sous-groupes dans lesquels lesdites orthèses finies qui constituent chaque dit sous-groupe affichent des surfaces supérieures façonnées sensiblement identiques ; et
(d) construire pour chacun de ladite pluralité de sous-groupes un moule à injection (30) ayant une cavité interne (30a) qui, lorsqu'elle est remplie d'un plastique moulable, produira une orthèse finie (14) ayant une surface supérieure façonnée substantiellement identique à la surface supérieure façonnée desdites orthèses (14) qui constituent chaque sous-groupe.
(a) identifier sur la surface supérieure façonnée de chaque dite orthèse fonctionnelle sélectionnée une multiplicité de coordonnées x, y ;
(b) pour chaque dite orthèse fonctionnelle sélectionnée, définir un plan couvrant ladite surface supérieure façonnée de celle-ci et espacé de celle-ci ; et
(c) pour chaque dite orthèse fonctionnelle sélectionnée, déterminer et enregistrer pour chaque coordonnée x, y identifiée sur celle-ci la distance entre la coordonnée et ledit plan, d'où il résulte que pour chaque dit moule à injection construit, un ensemble de données x, y, z peut être attribué à celui-ci, ledit ensemble de données x, y, z définissant le contour de la surface supérieure des orthèses fonctionnelles qui constituent le sous-groupe d'orthèses fonctionnelles pour lequel le moule a été fabriqué.
(a) identifier sur la surface inférieure façonnée de celle-ci une multiplicité de coordonnées x, y ;
(b) pour chaque dite réplique corrigée sélectionnée, définir un plan couvrant ladite surface inférieure façonnée de celle-ci et espacé de celle-ci ; et
(c) pour chaque dite réplique corrigée sélectionnée, déterminer et enregistrer pour chaque coordonnée x, y identifiée sur celle-ci la distance entre la coordonnée et ledit plan.
(a) identifier sur la surface inférieure façonnée de celle-ci une multiplicité de coordonnées x, y ;
(b) pour chaque dite réplique non corrigée sélectionnée, définir un plan couvrant ladite surface inférieure façonnée de celle-ci et espacé de celle-ci ; et
(c) pour chaque dite réplique non corrigée sélectionnée, déterminer et enregistrer pour chaque coordonnée x, y identifiée sur celle-ci la distance entre la coordonnée et ledit plan.
(a) identifier sur celle-ci une multiplicité de coordonnées x, y ;
(b) pour chaque dite impression de pied sélectionnée, définir un plan de base couvrant ladite impression de pied et espacé de celle-ci ; et
(c) pour chaque dite impression de pied sélectionnée, déterminer et enregistrer pour chaque coordonnée x, y identifiée sur celle-ci la distance entre la coordonnée et le plan de base.
(a) sélectionner une multiplicité de répliques non corrigées du pied humain, chacune ayant une surface inférieure façonnée non corrigée et dont chacune sera corrigée ultérieurement pour former une réplique corrigée ayant une surface façonnée corrigée à partir de laquelle une orthèse peut être fabriquée ;
(b) identifier une multiplicité de répliques corrigées fabriquées à partir de ladite multiplicité de répliques non corrigées ; et
(c) identifier la multiplicité d'orthèses fabriquées à partir de ladite multiplicité de répliques corrigées.
(a) identifier une pluralité de deuxièmes sous-groupes en divisant ladite multiplicité de répliques corrigées en deuxièmes sous-groupes dans lesquels lesdites répliques corrigées qui constituent chaque dit deuxième sous-groupe affichent des surfaces inférieures façonnées substantiellement identiques ;
(b) identifier une pluralité de troisièmes sous-groupes en identifiant pour chaque dit deuxième sous-groupe les répliques non corrigées qui ont été corrigées pour former lesdites répliques corrigées qui constituent ledit deuxième sous-groupe ;
(c) pour chaque dite réplique non corrigée de chacun de ladite pluralité de troisièmes sous-groupes :
(i) identifier sur la surface inférieure façonnée de celle-ci une multiplicité de coordonnées x, y ;
(ii) définir un plan couvrant ladite surface inférieure façonnée et espacé de celle-ci ; et
(iii) déterminer et enregistrer pour chaque coordonnée x, y identifiée sur chaque dite réplique non corrigée desdits troisièmes sous-groupes la distance entre la coordonnée et ledit plan.
(a) identifier sur celle-ci une multiplicité de coordonnées x, y ;
(b) pour chaque dite impression de pied individuelle sélectionnée, définir un plan de base couvrant ladite surface façonnée et espacé de celle-ci ; et
(c) pour chaque dite impression de pied individuelle sélectionnée, déterminer et enregistrer pour chaque coordonnée x, y identifiée sur chaque dite impression de pied individuelle sélectionnée la distance entre la coordonnée et le plan de base.
(i) sélectionner une multiplicité d'impressions du pied humain, chacune ayant une cavité ayant une surface façonnée laquelle cavité sera ultérieurement utilisée pour former une réplique non corrigée qui, elle-même, sera ultérieurement corrigée pour former une réplique corrigée ayant une surface façonnée corrigée à partir de laquelle une orthèse peut être formée ; et
(ii) identifier les orthèses fonctionnelles fabriquées à partir desdites répliques corrigées.
(a) identifier une pluralité de deuxièmes sous-groupes en divisant les répliques corrigées en deuxièmes sous-groupes dans lesquels lesdites répliques corrigées qui constituent chaque dit deuxième sous-groupe affichent des surfaces inférieures façonnées substantiellement identiques ;
(b) identifier une pluralité de troisièmes sous-groupes en identifiant pour chaque dit deuxième sous-groupe les répliques non corrigées qui ont été corrigées pour former lesdites répliques corrigées qui constituent ledit deuxième sous-groupe ;
(c) identifier une pluralité de sous-groupes d'impressions de pied en identifiant pour chaque sous-groupe les impressions de pied utilisées pour former lesdites répliques non corrigées qui constituent ledit troisième sous-groupe ;
(d) pour chaque dite impression de pied de chacun de ladite pluralité de sous-groupes d'impressions de pied :
(i) identifier sur la surface façonnée de la cavité de celle-ci une multiplicité de coordonnées x, y ;
(ii) définir un plan couvrant ladite surface façonnée et espacé de celle-ci ; et
(iii) déterminer et enregistrer pour chaque coordonnée x, y identifiée sur ladite surface façonnée la distance entre la coordonnée et ledit plan.
(e) formuler une pluralité d'ensembles de données de comparaison en déterminant pour chacun desdits sous-groupes d'orthèses la forme du contour des surfaces façonnées des impressions de pied et les répliques non corrigées qui ont été utilisées pour fabriquer les répliques corrigées qui, elles-mêmes, ont été utilisées pour former les orthèses qui constituent chacun desdits sous-groupes d'orthèses ;
(f) déterminer la forme du contour de la surface S'engageant avec la chaussure du pied du patient ;
(g) comparer ladite forme du contour de la surface s'engageant avec la chaussure du pied du patient ainsi déterminée avec lesdits ensembles de données de comparaison pour identifier les données de l'ensemble de comparaison qui définissent la forme des surfaces façonnées de ladite impression de pied et les répliques non corrigées qui correspondent au plus près à ladite forme du contour de la surface s'engageant avec la chaussure du pied du patient ;
(h) identifier ledit sous-groupe d'orthèses qui consiste en les orthèses formées à partir des répliques corrigées fabriquées à partir des répliques non corrigées qui affichent une forme de surface façonnée qui correspond aux formes définies dans l'ensemble identifié de données de comparaison ;
(i) sélectionner le moule à injection fabriqué pour ledit sous-groupe d'orthèses identifié ; et
(j) mouler à partir dudit moule sélectionné une orthèse finie pour le patient.
(a) identifier sur ladite surface façonnée une multiplicité de coordonnées x, y ;
(b) définir un plan de base couvrant ladite impression de pied et espacé de celle-ci ; et
(c) déterminer et enregistrer pour chaque coordonnée x, y identifiée sur celle-ci la distance entre la coordonnée et le plan de base.
(a) identifier sur ladite surface façonnée une multiplicité de coordonnées x, y ;
(b) définir un plan de base couvrant ladite surface façonnée et espacé de celle-ci ; et
(c) déterminer et enregistrer pour chaque coordonnée x, y identifiée sur celle-ci la distance entre la coordonnée et le plan de base.
(a) sélectionner une multiplicité de répliques corrigées (28) du pied humain, chacune ayant été fabriquée à partir d'une réplique non corrigée (26) d'un pied humain différent ayant une surface inférieure façonnée non corrigée, chaque dite réplique corrigée (28) affichant une surface inférieure façonnée corrigée à partir de laquelle une orthèse (14) peut être formée par chauffage et pressage d'une préforme thermoplastique contre celle-ci. ;
(b) examiner chaque dite réplique corrigée (28) de ladite multiplicité sélectionnée de répliques corrigées pour identifier celles ayant des surfaces inférieures façonnées substantiellement identiques ;
(c) identifier une pluralité de sous-groupes de répliques corrigées en groupant ladite multiplicité de répliques corrigées (28) qui ont été examinées en sous-groupes dans lesquels lesdites répliques corrigées (28) qui constituent chaque dit sous-groupe affichent des surfaces inférieures façonnées substantiellement identiques ;
(d) fabriquer pour chacun de ladite pluralité de sous-groupes un moule d'injection (30) ayant une cavité interne (30a) qui, lorsqu'elle est remplie d'un plastique moulable, produira une orthèse finie (14) ayant une surface supérieure façonnée substantiellement identique aux surfaces inférieures façonnées desdites répliques corrigées (28) qui constituent chaque dit sous-groupe ;
(e) formuler une pluralité d'ensembles de données de comparaison en déterminant pour chacun desdits sous-groupes de répliques corrigées la forme du contour des surfaces façonnées des impressions de pied et les répliques non corrigées (26) qui ont été utilisées pour fabriquer les répliques corrigées (28) qui constituent chacun desdits sous-groupes de répliques corrigées ;
(f) déterminer le contour de la surface d'engagement avec la chaussure du pied du patient ;
(g) comparer ledit contour de la surface d'engagement avec la chaussure du pied du patient ainsi déterminé avec lesdits ensembles de données de comparaison pour identifier l'ensemble particulier de données de comparaison qui définit la forme des surfaces façonnées de ladite impression de pied et les répliques non corrigées (26) qui correspondent au plus près à ladite forme du contour de la surface d'engagement avec la chaussure du pied du patient ;
(h) identifier le sous-groupe de répliques corrigées qui consiste en les répliques corrigées (28) fabriquées en utilisant les répliques non corrigées (26) qui affichent une forme de surface façonnée qui correspond aux formes définies dans l'ensemble identifié de données de comparaison ;
(i) sélectionner ledit moule d'injection (30) fabriqué pour ledit sous-groupe de répliques corrigées identifié; et
(j) mouler à partir dudit moule (30) sélectionné une orthèse finie (14) pour le patient.
(a) identifier sur ladite surface façonnée une multiplicité de coordonnées x, y ;
(b) définir un plan de base couvrant ladite impression de pied et espacé de celle-ci ; et
(c) déterminer et enregistrer pour chaque coordonnée x, y identifiée sur celle-ci la distance entre la coordonnée et le plan de base.
(a) identifier sur ladite surface façonnée une multiplicité de coordonnées x, y ;
(b) définir un plan de base couvrant ladite surface façonnée de ladite réplique non corrigée et espacé de celle-ci ; et
(c) déterminer et enregistrer pour chaque coordonnée x, y identifiée sur celle-ci la distance entre la coordonnée et le plan de base.
(a) sélectionner une multiplicité de répliques différentes du pied humain, dont chacune d'entre elles sera utilisée ultérieurement pour former selon des techniques classiques une réplique corrigée (28) ayant une surface façonnée corrigée à partir de laquelle une orthèse (14) peut être formée ;
(b) sélectionner une multiplicité de répliques corrigées (28) à partir de celles fabriquées à partir de ladite multiplicité de répliques sélectionnées du pied humain ;
(c) sélectionner une multiplicité d'orthèses fonctionnelles (14) à partir de celles fabriquées à partir de ladite multiplicité de répliques corrigées sélectionnées (28) ;
(d) identifier une pluralité de premiers sous-groupes en examinant chaque dite orthèse fonctionnelle (14) de ladite multiplicité d'orthèses fonctionnelles sélectionnées pour identifier les orthèses fonctionnelles ayant une surface supérieure façonnée substantiellement identique ;
(e) produire une multiplicité de moules d'injection (30) en fabriquant pour chacun de ladite pluralité de premiers sous-groupes un moule d'injection (30) ayant une cavité interne (30a) qui, lorsqu'elle est remplie d'un plastique moulable, produira une orthèse finie (14) ayant une surface supérieure façonnée substantiellement identique à la surface supérieure façonnée desdites orthèses fonctionnelles (14) qui constituent chaque dit sous-groupe ;
(f) identifier une pluralité de deuxièmes sous-groupes en divisant ladite multiplicité de répliques corrigées (28) sélectionnées en deuxièmes sous-groupes dans lesquels lesdites répliques corrigées (28) qui constituent chaque dit deuxième sous-groupe affichent des surfaces inférieures façonnées substantiellement identiques ;
(g) identifier une pluralité de troisièmes sous-groupes en identifiant pour chaque dit deuxième sous-groupe les répliques non corrigées (26) qui ont été corrigées pour former lesdites répliques corrigées (28) qui constituent ledit deuxième sous-groupe ;
(h) produire un premier ensemble de données de comparaison en analysant ladite pluralité desdits troisièmes sous-groupes de répliques non corrigées (26) et pour chaque dite réplique non corrigée (26) de chacun de ladite pluralité desdits troisièmes sous-groupes :
(i) identifier sur la surface inférieure façonnée de celle-ci une multiplicité de coordonnées x, y ;
(ii) définir un plan de référence couvrant ladite surface inférieure façonnée et espacé de celle-ci ;
(iii) déterminer et enregistrer pour chaque coordonnée x, y identifiée sur chaque dite réplique non corrigée (26) desdits troisièmes sous-groupes la distance entre la coordonnée et ledit plan de référence ;
(i) déterminer et enregistrer les données x, y, z pour la surface inférieure façonnée du pied du patient en déterminant, pour chacune d'une multiplicité de coordonnées x, y définie sur ladite surface inférieure façonnée de celui-ci, la hauteur de la coordonnée au dessus d'un plan de référence pour développer les données x, y, z du patient ;
(j) comparer lesdites données x, y, z du patient avec lesdits groupes de comparaison de données x, y, z pour identifier le groupe de comparaison de données x, y, z dans lequel tombent lesdites données x, y, z du patient ;
(k) sélectionner ledit moule injection (30) qui correspond audit groupe de comparaison sélectionné de données x, y, z ; et
(l) mouler à partir dudit moule à injection sélectionné (30) l'orthèse finie (14).